ORCID Profile
0000-0002-8021-6818
Current Organisation
UNSW Sydney
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Publisher: American Chemical Society (ACS)
Date: 16-08-2022
Publisher: Elsevier BV
Date: 12-2021
Publisher: Wiley
Date: 20-09-2022
Abstract: To reduce the reliance on fossil fuel, H 2 , as a clean fuel, has attracted substantial research and development activities in recent years. The traditional water splitting approach requires an applied bias of more than 1.5 V and the use of ion‐selective membranes to prevent the formation of a potentially explosive H 2 –O 2 gas mixture, resulting in increased cost and system design complexity. Here, a solar‐driven H 2 production process requiring a much lower applied bias of 1.05 V is reported whereby aniline (ANI) is oxidized to polyaniline (PANI) at the anode with a yield of 96% and H 2 evolution reaction occurs at the cathode with a faradaic efficiency of 98.6 ± 3.9%. The process has multiple advantages including the elimination of ion‐exchange membrane as PANI is a solid product that also is of substantially higher value than O 2 . For demonstration, a single junction perovskite solar cell and low‐cost earth abundant CoP catalyst are successfully applied for this process. This process contributes to the advancement of solar‐driven low‐cost H 2 generation coupled with co‐production of a high‐value product expediting the transition to a hydrogen economy.
Publisher: American Physical Society (APS)
Date: 19-07-2007
Publisher: Springer Science and Business Media LLC
Date: 29-04-2015
Publisher: American Chemical Society (ACS)
Date: 16-11-2023
Publisher: American Association for the Advancement of Science (AAAS)
Date: 06-06-2008
Abstract: Atomic quantum gases in the strong-correlation regime offer unique possibilities to explore a variety of many-body quantum phenomena. Reaching this regime has usually required both strong elastic and weak inelastic interactions because the latter produce losses. We show that strong inelastic collisions can actually inhibit particle losses and drive a system into a strongly correlated regime. Studying the dynamics of ultracold molecules in an optical lattice confined to one dimension, we show that the particle loss rate is reduced by a factor of 10. Adding a lattice along the one dimension increases the reduction to a factor of 2000. Our results open the possibility to observe exotic quantum many-body phenomena with systems that suffer from strong inelastic collisions.
Publisher: AIP Publishing
Date: 03-2023
DOI: 10.1063/5.0117424
Abstract: Epitaxial monolithic III–V/Si tandem solar cells are one of the most promising technologies to be adopted by the industry after the efficiency of the current market dominating single junction silicon solar cell saturates at its fundamental limit. One of the key limitations of this technology is the degradation of silicon wafers during in situ annealing in the molecular beam epitaxy chamber. Determining the nature of contaminants in this process is key to improve the efficiency of epitaxial tandem solar cells. However, to date, the nature of contaminants from molecular beam epitaxy chambers remains unknown. In this work, we use photoluminescence imaging, lifetime spectroscopy, and deep level transient spectroscopy to measure the electronic properties of extrinsic impurities incorporated during annealing in the molecular beam epitaxy chamber. Photoluminescence images reveal that at least two impurities diffuse into silicon wafers during molecular beam epitaxy annealing. One is highly localized, while the other one is distributed uniformly across the whole wafer. Phosphorus diffusion is found to confine the localized impurity within the diffused layer but is ineffective at preventing the indiffusion of other impurities. Lifetime spectroscopy shows that metastable impurities with characteristic similar to Cr and CrB in our molecular beam epitaxy annealed silicon wafers. No evidence of Fe or FeB was observed. The emission rates and concentrations of the electrically active defects were measured with deep-level transient spectroscopy: The emission rates of detected defects do not match that of known Cr-related defects.
Publisher: Springer Science and Business Media LLC
Date: 30-05-2014
Publisher: Wiley
Date: 02-08-2022
Abstract: High bandgap perovskite solar cells are integral to perovskite‐based multi‐junction tandem solar cells with efficiency potentials over 40%. However, at present, high bandgap perovskite devices underperform compared to their mid bandgap counterparts in terms of voltage outputs and fill factors resulting in lower than ideal efficiencies. Here, the low fill factor aspect of high bandgap perovskite is addressed by developing a cation‐diffusion‐based double‐sided interface passivation scheme that simultaneously provides bulk passivation for a 1.75 eV perovskite cell that is also compatible with a p‐i‐n cell architecture. The ch ion cell achieves a record fill factor of 86.5% and a power conversion efficiency of 20.2%. Results of ionic distribution profiling, Fourier transform infrared spectroscopy, and X‐ray diffraction crystallography reveal evidence of cation diffusion from the surface perovskite passivation layer into bulk. The diffused cations reduce Shockley–Read–Hall recombination in the perovskite bulk and at the surfaces with the latter being more dominant as confirmed by light‐intensity dependent and temperature‐dependent open‐circuit voltage measurements as well as thermal admittance spectroscopy. This concurrent bulk and surface passivation scheme renders record fill factor and efficiency in the double‐side passivated cells. This provides new insights for future passivation strategies based on ionic diffusion of functionalized materials.
No related grants have been discovered for Daniel Dietze.